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Hello,
In minimap the -G
parameter decides the maximum gap on the reference during spliced alignments. So I take this as either intron length or intergenic length. Is my assumption correct? This is set to 200000 by default. I set the -G
value to 50000 for my species, as the 90th percentile value of intron length was 48000. It turns out that the gene I was interested in had a single 60000 bp intron. Therefore, FLNC reads that should have aligned did not, as I set -G 50000
. When I ran minimap with default -G
the reads aligned fine. Therefore, a few questions.
- Is it advisable to reduce this size closer to the anticipated intron size of a species?
- How strictly does the tool adhere to the
-G
parameter value? You mention that this has an effect on the chaining and alignment band width. Which are these parameters? and what do they control?
Thanks
Abhijit
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